http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1009015-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-40
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-40
filingDate 1962-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b853947d26083a2b0612fbbad53ddc4e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be3d433007b7e78009011ddc5c2092f5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a66e0e8f14430a8d8794f96a0c0193bd
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publicationDate 1965-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1009015-A
titleOfInvention Improvements in or relating to substituted imidazolidinones
abstract The invention comprises 4,5-dialkenyloxy-2-imidazolidinones of formula <FORM:1009015/C2/1> where R is an alkenyl radical having 3 to 6 carbon atoms, and their preparation by heating 4,5 - dihydroxy - 2 - midazolidinone with an unsaturated aliphatic alcohol in the presence of a solid inorganic salt as a dehydrating agent. Dehydrating agents specified are anhydrous zinc chloride, anhydrous copper sulphate, dried copper sulphate monohydrate, anhydrous magnesium sulphate and anhydrous calcium sulphate. The compounds of the invention depress the central nervous system, having sedative, tranquillizing, hypnotic and anticonvulsant activity, and may be used in pharmaceutical compositions in combination with a carrier, e.g. in forms suitable for oral or parenteral administration, such as tablets, coated tablets, granules, solutions or suspensions.
priorityDate 1962-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 25.